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A cluster-randomized trial to reduce cesarean delivery rates in Quebec.
Chaillet N, Dumont A, Abrahamowicz M, Pasquier JC, Audibert F, Monnier P, Abenhaim HA, Dubé E, Dugas M, Burne R, Fraser WD; QUARISMA Trial Research Group. Chaillet N, et al. Among authors: audibert f. N Engl J Med. 2015 Apr 30;372(18):1710-21. doi: 10.1056/NEJMoa1407120. N Engl J Med. 2015. PMID: 25923551 Free article. Clinical Trial.
Nipocalimab in Early-Onset Severe Hemolytic Disease of the Fetus and Newborn.
Moise KJ Jr, Ling LE, Oepkes D, Tiblad E, Verweij EJTJ, Lopriore E, Smoleniec J, Sachs UJ, Bein G, Kilby MD, Miller RS, Devlieger R, Audibert F, Emery SP, Markham K, Norton ME, Ocón-Hernández O, Pandya P, Pereira L, Silver RM, Windrim R, Streisand JB, Leu JH, Mirza A, Smith V, Schwartz LB, Tjoa ML, Saeed-Khawaja S, Komatsu Y, Bussel JB; UNITY Study Group. Moise KJ Jr, et al. Among authors: audibert f. N Engl J Med. 2024 Aug 8;391(6):526-537. doi: 10.1056/NEJMoa2314466. N Engl J Med. 2024. PMID: 39115062 Clinical Trial.
Development and validation of a prognostic model to predict birth weight: individual participant data meta-analysis.
Allotey J, Archer L, Snell KIE, Coomar D, Massé J, Sletner L, Wolf H, Daskalakis G, Saito S, Ganzevoort W, Ohkuchi A, Mistry H, Farrar D, Mone F, Zhang J, Seed PT, Teede H, Da Silva Costa F, Souka AP, Smuk M, Ferrazzani S, Salvi S, Prefumo F, Gabbay-Benziv R, Nagata C, Takeda S, Sequeira E, Lapaire O, Cecatti JG, Morris RK, Baschat AA, Salvesen K, Smits L, Anggraini D, Rumbold A, van Gelder M, Coomarasamy A, Kingdom J, Heinonen S, Khalil A, Goffinet F, Haqnawaz S, Zamora J, Riley RD, Thangaratinam S; International Prediction of Pregnancy Complications collaborative network; Kwong A, Savitri AI, Bhattacharya S, Uiterwaal CS, Staff AC, Andersen LB, Olive EL, Redman C, Macleod M, Thilaganathan B, Ramírez JA, Audibert F, Magnus PM, Jenum AK, McAuliffe FM, West J, Askie LM, Zimmerman PA, Riddell C, van de Post J, Illanes SE, Holzman C, van Kuijk SMJ, Carbillon L, Villa PM, Eskild A, Chappell L, Velauthar L, van Oostwaard M, Verlohren S, Poston L, Ferrazzi E, Vinter CA, Brown M, Vollebregt KC, Langenveld J, Widmer M, Haavaldsen C, Carroli G, Olsen J, Zavaleta N, Eisensee I, Vergani P, Lumbiganon P, Makrides M, Facchinetti F, Temmerman M, Gibson R, Frusca T, Norman JE, Figueiró-Fi… See abstract for full author list ➔ Allotey J, et al. Among authors: audibert f. BMJ Med. 2024 Aug 14;3(1):e000784. doi: 10.1136/bmjmed-2023-000784. eCollection 2024. BMJ Med. 2024. PMID: 39184566 Free PMC article.
Bi-allelic variants in MYH3 cause recessively-inherited arthrogryposis.
Morali B, Miranda V, Raelson J, Grimard G, Glavas P, Audibert F, Dumont NA, Barone J, Bamshad M, Lemyre E, Campeau PM. Morali B, et al. Among authors: audibert f. Clin Genet. 2024 Oct;106(4):483-487. doi: 10.1111/cge.14570. Epub 2024 Jun 10. Clin Genet. 2024. PMID: 38856159
380 results